Review Article

The Beneficial Effects of Probiotics via Autophagy: A Systematic Review

Table 2

The effects of probiotics on different tissues in animal models via autophagy.

ProbioticsTissue/diseaseOutcomesReferences

Bifidobacterium breveIntestineProbiotics modify protein degradation programs within the intestinal epithelial cells to promote their survival during stress.[26]
BacillusIntestineProbiotics improved growth performance via increasing intestinal autophagy.[36]
LactobacillusIntestinal injury gastroenteritisProbiotics reduced autophagy marker expression to normal levels and partially prevented virus-induced tissue damage.[11]
L. plantarum, B. and S. cerevisiaeIntestineProbiotic feeding improved the growth, immune function, and intestinal health in weaned piglets.[37]
Bacillus (SC06 or SC080IntestineBacillus SC06 alleviated oxidative stress-induced disorders and apoptosis via p38-mediated autophagy.[28]
LactobacillusIntestineProbiotics supplementation protected LPS-induced intestinal barrier dysfunction via attenuating apoptosis and autophagy via mTOR signaling pathway.[35]
B. dentiumIntestineProbiotics enhanced the intestinal mucus layer and goblet cell function via upregulation of gene expression and autophagy signaling pathways.[27]
LABIntestineProbiotics caused anti-infection and anti-inflammation via inducing autophagy.[30]
Lactobacillus rhamnosus, Pediococcus acidilactici, Bifidobacterium adolescentisCardiac tissueOral administration of probiotics provided cardiac protection via regulation of fibrosis and autophagy.[40]
SLAB51Alzheimer diseasePrebiotic treatment by activating autophagy decreased the brain damage and cognitive decline in Alzheimeric mice.[46]
Short-chain fatty acids (SCFAs) are produced by the intestinal microbiotaKidneySCFAs improved the renal dysfunction caused by injury. This protection was partially associated with an increase in autophagy.[51]
ZJ617LiverZJ617s exerted beneficial effects on the mouse liver through suppression of hepatic TLR4/MAPK/NF-κB activation and autophagy.[55]
Golden bifidPlacentaOral supplementation with golden bifid induced placental protection via reducing the autophagy-related protein Beclin1.[38]
Lactobacillus rhamnosusZebrafishParental Lactobacillus rhamnosus administration can modulate important physiological processes involved in zebrafish embryo development.[19]
Lactobacillus rhamnosusOvarian folliclesProbiotics modulated the balance between apoptosis and autophagy and improved the follicular survival.[39]
Lactobacillus salivarius AR809Pharyngeal epitheliumAR809 prevents S. aureus-induced pharyngeal inflammatory response, possibly by regulating mTOR signaling pathway-related autophagy.[56]

SLAB51: a formulation made of nine live bacterial strains [Streptococcus thermophilus, Bifidobacteria (B. longum, B. breve, B. infantis), Lactobacillus (L. acidophilus, L. plantarum, L. paracasei, L. delbrueckii subsp. bulgaricus, L. brevis)]; LAB: lactic acid bacteria; ZJ617: Lactobacillus reuteri.